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340,000+ productos de investigación · Triple ISO certified · COA & SDS Disponible para cada producto · Envío el mismo día para artículos en stock Terpineol - ≥95%, mixture of isomers , CAS No.8000-41-7
GRADE & PURITY ≥95% mixture of isomers Synonyms
2-(4-methylcyclohex-3-en-1-yl)propan-2-ol | p-Menth-1-en-8-ol
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Why this grade ≥95%, mixture of isomers for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature Ships Normal Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 174 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Sinónimos
2-(4-methylcyclohex-3-en-1-yl)propan-2-ol | p-Menth-1-en-8-ol
Especificaciones y pureza
≥95%, mixture of isomers
Condiciones de almacenamiento de almacenamiento
Room temperature
Nombres e identificadores Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/504752800
Sonrisas canónicas
CC1=CCC(CC1)C(C)(C)O
IUPAC Name
2-(4-methylcyclohex-3-en-1-yl)propan-2-ol
InChIKey
WUOACPNHFRMFPN-UHFFFAOYSA-N
INCHI
1S/C10H18O/c1-8-4-6-9(7-5-8)10(2,3)11/h4,9,11H,5-7H2,1-3H3
Isómeros SMILES
CC1=CCC(CC1)C(C)(C)O
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1906604&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Lipids and lipid-like molecules Clase Prenol lipids Subclass Monoterpenoids Intermediate Tree Nodes Not available Direct Parent Menthane monoterpenoids Alternative Parents Monocyclic monoterpenoids Tertiary alcohols Hydrocarbon derivatives Molecular Framework Aliphatic homomonocyclic compounds Substituents P-menthane monoterpenoid - Monocyclic monoterpenoid - Tertiary alcohol - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Alcohol - Aliphatic homomonocyclic compound Descripción This compound belongs to the class of organic compounds known as menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes. External Descriptors a monoterpenol Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Estructura 3D Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Solubilidad Miscible with organic solvents. Slightly miscible with water. Sensibilidad Moisture sensitive. Índice de refracción 1.484 Punto de inflamación (°F) 190.4 °F Punto de inflamación (°C) 88 °C Punto de ebullición (°C) 213-218℃ Punto de fusión (°C) 31-36℃ Peso molecular 154.250 g/mol XLogP3 1.800 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 1 Rotatable Bond Count 1 Exact Mass 154.136 Da Monoisotopic Mass 154.136 Da Topological Polar Surface Area 20.200 Ų Heavy Atom Count 11 Formal Charge 0 Complexity 168.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 1 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
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